A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112771



Internal ID21296037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370534..115385420hg38UCSC Ensembl
Innerchr5:114706231..114721117hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3814887
hg1914887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv984n145
Supporting Variantsnssv14097343, nssv14109405, nssv14082689, nssv14109101, nssv14109003, nssv14097453, nssv14096784, nssv14082598, nssv14109057, nssv14108432
Samplessample145, sample123, sample241, sample95, sample41, sample375, sample227, sample210, sample335, sample398
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112771
Frequency
Sample Size467
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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